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Catalog Number:
24969
CAS Number:
23779-96-6
4-Hidroxi-8-(trifluorometil)quinolina
Purity:
≥ 99 % (HPLC)
Synonym(s):
8-(trifluorometil)-4-quinolinol
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Product Information

4-Hydroxy-8-(trifluoromethyl)quinoline is a versatile compound known for its unique trifluoromethyl group, which enhances its chemical stability and lipophilicity. This property makes it particularly valuable in pharmaceutical research, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its hydroxyl group contributes to its potential as a ligand in coordination chemistry, enabling the formation of metal complexes that can be utilized in catalysis and materials science.

In addition to its applications in drug development, 4-Hydroxy-8-(trifluoromethyl)quinoline has shown promise in agrochemical formulations, where it can act as a fungicide or herbicide due to its ability to disrupt biological processes in target organisms. Researchers appreciate its effectiveness in enhancing the efficacy of existing compounds, making it a valuable addition to any laboratory focused on innovative chemical solutions. With its broad range of applications, this compound is an essential tool for professionals seeking to advance their projects in medicinal chemistry and agricultural science.

Synonyms
8-(trifluorometil)-4-quinolinol
CAS Number
23779-96-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H6F3NO
Molecular Weight
213.16
MDL Number
MFCD00134577
PubChem ID
90261
Melting Point
171-177 ?C
Appearance
Polvo amorfo de color blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
8-(trifluorometil)-4-quinolinol
CAS Number
23779-96-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H6F3NO
Molecular Weight
213.16
MDL Number
MFCD00134577
PubChem ID
90261
Melting Point
171-177 ?C
Appearance
Polvo amorfo de color blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Hydroxy-8-(trifluoromethyl)quinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections and cancer. Its unique structure enhances biological activity, making it a valuable asset in drug discovery.
  • Fluorescent Probes: Due to its fluorescent properties, it is used in the development of probes for biological imaging. Researchers can use these probes to visualize cellular processes in real-time, aiding in the study of disease mechanisms.
  • Analytical Chemistry: It acts as a reagent in analytical methods, particularly in the detection of metal ions. This application is crucial for environmental monitoring and quality control in various industries.
  • Material Science: The compound is explored for its potential in creating advanced materials, such as coatings and polymers, that require specific optical or electronic properties, enhancing product performance.
  • Agricultural Chemistry: It is being investigated for use in agrochemicals, particularly as a fungicide or herbicide, providing an eco-friendly alternative to traditional chemicals while maintaining efficacy.

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